4-[(1S,3aS,6R,6aR)-3a,6-dihydroxyhexahydrofuro[3,4-c]furan-1-yl]-2-methoxyphenyl acetate

Base Information

Chemical Name:4-[(1S,3aS,6R,6aR)-3a,6-dihydroxyhexahydrofuro[3,4-c]furan-1-yl]-2-methoxyphenyl acetate
CAS No.:1186656-09-6
Molecular Formula:C₁₅H₁₈O₇
Molecular Weight:310.304
Hs Code.:

Synonyms:4-[(1S,3aS,6R,6aR)-3a,6-dihydroxyhexahydrofuro[3,4-c]furan-1-yl]-2-methoxyphenyl acetate

Suppliers and Price of 4-[(1S,3aS,6R,6aR)-3a,6-dihydroxyhexahydrofuro[3,4-c]furan-1-yl]-2-methoxyphenyl acetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 4-[(1S,3aS,6R,6aR)-3a,6-dihydroxyhexahydrofuro[3,4-c]furan-1-yl]-2-methoxyphenyl acetate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-[(1S,3aS,6R,6aR)-3a,6-dihydroxyhexahydrofuro[3,4-c]furan-1-yl]-2-methoxyphenyl acetate

There total 1 articles about 4-[(1S,3aS,6R,6aR)-3a,6-dihydroxyhexahydrofuro[3,4-c]furan-1-yl]-2-methoxyphenyl acetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 67.0%

: 62147-49-3
1,3-dihydroxyacetone dimer

: 65401-83-4
4-acetoxy-3-methoxycinnamaldehyde

: 1186656-09-6
4-[(1S,3aS,6R,6aR)-3a,6-dihydroxyhexahydrofuro[3,4-c]furan-1-yl]-2-methoxyphenyl acetate

Guidance literature:: With (2S)-2-{diphenyl[(trimethylsilyl)oxy]methyl}pyrrolidine; benzoic acid; In chloroform; at 20 ℃; optical yield given as %ee; enantioselective reaction;
DOI:10.1002/anie.200901333